Canonical Allele Identifier: CA2188861685

Gene: PSTPIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.77032940G= , CM000677.2:g.77032940G=	GRCh38
NC_000015.9:g.77325281G= , CM000677.1:g.77325281G=	GRCh37
NC_000015.8:g.75112336G=	NCBI36
NG_007526.1:g.42817G= , LRG_172:g.42817G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000697622.1:n.2083G=
ENST00000697623.1:n.2336G=
ENST00000558012.6:c.917G= MANE Select	ENSP00000452746.1:p.Gly306=
ENST00000379595.7:c.917G=	ENSP00000368914.3:p.Gly306=
ENST00000557995.1:n.581G=
ENST00000558012.5:c.917G=	ENSP00000452746.1:p.Gly306=
ENST00000558870.1:c.78+546G=
ENST00000559295.5:c.872+512G=	ENSP00000452743.1:n.872+512G=
ENST00000559785.5:c.1146G=	ENSP00000452986.1:p.Arg382=
ENST00000560223.5:c.*1019G=	ENSP00000454118.1:n.*1019G=
NM_003978.3:c.917G= , LRG_172t1:c.917G=	NP_003969.2:p.Gly306=
XM_006720737.2:c.551G=	XP_006720800.1:p.Gly184=
XM_011522163.1:c.974G=	XP_011520465.1:p.Gly325=
XM_011522164.1:c.872G=	XP_011520466.1:p.Gly291=
XM_011522165.1:c.770G=	XP_011520467.1:p.Gly257=
XM_011522166.1:c.1008G=	XP_011520468.1:p.Arg336=
XM_011522167.1:c.895+546G=	XP_011520469.1:n.895+546G=
XM_011522168.1:c.974G=	XP_011520470.1:p.Gly325=
XM_011522169.1:c.798+1662G=	XP_011520471.1:n.798+1662G=
XM_011522170.1:c.372-2568G=	XP_011520472.1:n.372-2568G=
XM_011522171.1:c.312-2568G=	XP_011520473.1:n.312-2568G=
XM_011522172.1:c.312-2568G=	XP_011520474.1:n.312-2568G=
XM_011522173.1:c.312-2568G=	XP_011520475.1:n.312-2568G=
XR_931936.1:n.1458G=
XR_931937.1:n.1401G=
XR_931938.1:n.1345+546G=
XR_931939.1:n.1248+1662G=
XR_931940.1:n.1070-2568G=
NM_001321135.1:c.872+512G=	NP_001308064.1:n.872+512G=
NM_001321136.1:c.890G=	NP_001308065.1:p.Gly297=
NM_001321137.1:c.1112G=	NP_001308066.1:p.Gly371=
NM_003978.4:c.917G=	NP_003969.2:p.Gly306=
NR_135552.1:n.1150+1662G=
XM_006720737.3:c.551G=	XP_006720800.1:p.Gly184=
XM_011522163.2:c.974G=	XP_011520465.1:p.Gly325=
XM_011522165.2:c.770G=	XP_011520467.1:p.Gly257=
XM_011522166.2:c.1008G=	XP_011520468.1:p.Arg336=
XM_011522167.2:c.895+546G=	XP_011520469.1:n.895+546G=
XM_011522168.3:c.974G=	XP_011520470.1:p.Gly325=
XM_011522169.2:c.798+1662G=	XP_011520471.1:n.798+1662G=
XR_931936.2:n.1456G=
XR_931937.2:n.1399G=
XR_931938.2:n.1343+546G=
XR_931939.2:n.1246+1662G=
NM_001321135.2:c.872+512G=	NP_001308064.1:n.872+512G=
NM_001321136.2:c.890G=	NP_001308065.1:p.Gly297=
NM_003978.5:c.917G= MANE Select	NP_003969.2:p.Gly306=
NR_135552.2:n.1109+1662G=